holocarboxylase synthetase deficiency (Q5883885)
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human disease
- Biotin-(propionyl-CoA-carboxylase) ligase deficiency (disorder)
- Multiple carboxylase deficiency - neonatal onset (disorder)
- Multiple carboxylase deficiency - neonatal onset
- Biotin-(propionyl-CoA-carboxylase) ligase deficiency
- Holocarboxylase Synthetase Deficiency
- Multiple Carboxylase Deficiency, Neonatal Form
- Neonatal Multiple Carboxylase Deficiency
- Multiple Carboxylase Deficiency
- Early-onset multiple carboxylase deficiency
- Hlcs Deficiency
- Multiple Carboxylase Deficiency, Early Onset
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | holocarboxylase synthetase deficiency |
human disease |
|
Statements
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1 reference
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270.8
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1 reference
Identifiers
Holocarboxylase Synthetase Deficiency
1 reference
1 reference
2 references
2 references
1 reference
1 reference